Hey Ming Tang,
Thanks for your answer.
I'm sorry for the late reply but I wanted to read the article you sent me before replying.
So I read it and I also read about PLS then I have two questions that come to me that you might have an answer to:
- Since you are working on a scRNAseq sample, i assume that there is a lot of sparsity. So why did not you use a (s)PLS-DA instead of a classical PLS-DA?
- I saw that when we work with PLS method, we must verify the linearity of the data. I am not sure that you verify this part in your article, have you verified it on your side and not mentioned it into the article.
PS: Great blog by the way!